Have a personal or library account? Click to login

Correction with thiocetam of lead nanoparticles influence on morpho-functional status of rat liver

Open Access
|Sep 2020

References

  1. 1. Özdemir-Kumral ZN, Erkek BE, Karakuş B, Almacı M, Fathi R, Yüksel M, et al. Potential effect of 1,25 dihydroxyvitamin D3 on thioacetamide-induced hepatotoxicity in rats. J Surg Res. 2019;6(243):165-72.10.1016/j.jss.2019.05.020
  2. 2. Omelchuk ST, Aleksijchuk VD, Sokurenko LM, Blagaia A, Prudchenko S. Characteristics of rat liver exposed to nanoparticles of lead compounds. Georgian Med News. 2016;261:94-9.
  3. 3. Sahlman P, Nissinen M, Puukka P, Jula A, Salomaa V, Männistö S, et al. Genetic and life-style risk factors for advanced liver disease among men and women. J Gastroenterol Hepatol. 2020:35(2):291-8.10.1111/jgh.14770
  4. 4. Gumeny uk AV, Motorna N V, Ryba lko SL, Savosko SI, Sokurenko LM, Chaikovsky YuB. Mutual influence of herpes virus infection activation and cerebral circulation impairment on the state of brain cells. Biopolym Cell. 2016;32(2):126-30.10.7124/bc.000915
  5. 5. Motorna N, Rybalko S, Kvitnitskaya-Ryzhova T, Starosyla D, Strokina I, Kaminsky R, et al. Ultrastructural changes in murine liver following HSV infection and stroke. Ultrastructural changes in murine liver following HSV infection and stroke. Curr Issues Pharm Med Sci. 2018;31(1):10-2.10.1515/cipms-2018-0002
  6. 6. Motorna NV, Rybalko SL, Sokurenko LM, Starosyla DB, Savosko SI, Chaikovsky YuB. Patterns of herpetic infection reactivation in the liver. Mikrobiol Z. 2017;79(5):70-9.10.15407/microbiolj79.05.070
  7. 7. Khan HA, Ahmad MZ, Khan JA, Arshad MI. Crosstalk of liver immune cells and cell death mechanisms in different murine models of liver injury and its clinical relevance. Hepatobiliary Pancreat Dis Int. 2017;16(3):245-56.10.1016/S1499-3872(17)60014-6
  8. 8. Campana L, Iredale JP. Regression of Liver Fibrosis. Semin Liver Dis. 2017;37(1):1-10.10.1055/s-0036-159781628201843
  9. 9. Hou XJ, Ye F, Li XY, Liu WT, Jing YY, Han ZP, Wei LX. Immune response involved in liver damage and the activation of hepatic progenitor cells during liver tumorigenesis. Cell Immunol. 2018;326: 52-9.10.1016/j.cellimm.2017.08.00428860007
  10. 10. Sokurenko LM, Chaikovskii YuB. Mildronate protects neuroblasts against toxic inf luence of mercuric chloride in cell culture. Neurophysiology. 2014;46(3):271-3.10.1007/s11062-014-9440-7
  11. 11. Kamynsky R, Primachenko V, Sokurenko L, Chaikovsky Y. A study of impact of mercury chloride on myocardium in experiment. Georgian Med News. 2016;251:64-70.
  12. 12. Lavrinenko VE, Zinabadinova SS, Shobat LB, Sokurenko LM, Chaikovsky YuB. Influence of nanodiamonds and carbon nanowires on survival and cells structure in chicken embryo. Georgian Med News. 2016;6(255):93-9.
  13. 13. Hardman R. A toxicologic review of quantum dots: toxicity depends on physicochemical and environmental factors. Environ Health Perspect. 2006;114(2):165-72.10.1289/ehp.8284136782616451849
  14. 14. Demetskaya AV, Kucheruk TK, Movchan VA. Nanoscale particles: possible contribution to the development of occupational pathology. Ukr J Healthcare Prof. 2006;1:62-7.10.33573/ujoh2006.01.062
  15. 15. Dmy truk ha SP, Luhovsky OS, Lahutina NM. Evaluation of immunotoxic effect of lead compounds with micro-and nanoparticles. Mod Prob Tox Food Chem Saf. 2014;1-2(77-78):60-6.10.1016/j.ejsobi.2013.11.006
  16. 16. Lugovskyi S, Didenko М, Melnyk N. Morpho-functional changes in rats’ inner organs under chronic effect of micro and nano of inorganic compounds of lead for undamaged skin. Mod Prob Tox Food Chem Saf. 2017;3:34-47.
  17. 17. Prodanchuk NG, Balan GM. Nanotoxicology: status and prospects of research. Curr Probl Tox. 2009;(3-4):4-18.
  18. 18. Balan GM, Yurchenko IV, Ignatenko LV. To the clinic and treatment of neurological and abdominal disorders in chronic lead intoxication. Curr Prob Tox. 2003;4:58-62.
  19. 19. Apikhtina OL. Investigation of the membrane-toxic effect of heavy metals on a model of blood red blood cells in vitro. Curr Probl Tox. 2011;1-2:65-9.
  20. 20. Kasperczyk S, Birkner E, Kasperczyk A, Zalejska-Fiolka J. Activity of superoxide dismutase and catalase in people protractedly exposed to lead compounds. Ann Agric Environ Med. 2004;11(2):291-6.
  21. 21. Petrynych VV, Vlasyk LI, Petrynych OA. Lead: toxicological, hygienic and biological aspects. Сlin Exper Path. 2017;16(60):97-102.10.24061/1727-4338.XVI.2.60.2017.20
  22. 22. Aleksiichuk V, Omelchuk S, Sokurenko L, Kaminsky R, Kovalchuk O, Chaikovsky Y. The influence of lead nanoparticles on the morpho-functional changes of rat liver during the postexposure period. Microsc Res Tech. 2018;81:781-8.10.1002/jemt.2303629652104
  23. 23. Mazur IA, Chekman IS, Belenichev IF. Metabolitotropic drugs. Zaporizhia; 2007:309.
  24. 24. Sokurenko LM, Savchyna MO, Litus VI, Kaminsky RF, Сhaikovsky YB. Rat spinal ganglia in assessment of protective action of antioxidants: A morphological study. Medicina (Kaunas). 2017;53(4):217-23.10.1016/j.medici.2017.11.00129273287
  25. 25. Kaminsky RF, Sokurenko LM, Chaikovsky YB. Status of rats myocardium under subchronic mercury exposure and its pharmacological correction. Curr Issues Pharm Med Sci. 2016;29(4): 167-70.10.1515/cipms-2016-0035
  26. 26. Mazur IA, Voloshin ON, Chekman IS. Thiotriazolin. Zaporozhye-Lviv; 2005:156.
  27. 27. Sokurenko LM, Chaikovskii YuB. Protective effects of Thiotriazolinum and Mildronate against mercury chloride toxicity in neuroblastoma cell culture. Neurophysiology. 2016;48(3):171-5.10.1007/s11062-016-9585-7
  28. 28. Karnauk h EV. Piracetam: morphofunctional antistress cardioprotection according to electron microscopy. Medicine Today Tomorrow. 2011;3(52):28-32.
  29. 29. Motorna NV, Rybalko SL, Starosyla DB, Guzyk MM, Strokina IG, Kaminsky RF, et al. The study of leukocyte phagocytic activity in the presence of herpetic infection and stroke. Wiad Lek. 2018;71 (1 pt 2):155-9.
  30. 30. Zakharash AD, Dieltsova OI. Systemic manifestations of membrane-damaging inf luence in patients with chronic hepatitis with cholestasis syndrome. Herald Morph. 2011;17(1):120-5.
  31. 31. Kunneva VS, Koltunova IG. Pectins of various degrees of esterification and pectin containing drug “Medopect” as factors contributing to the elimination of lead from the body (experimental data). Labor Med Indust Ecol. 1997;7:27-31.
  32. 32. Omelchuk ST, Aleksiĭchuk VD, Sokurenko LM. Biochemical parameters of blood and morpho-functional state of the liver of experimental animals by the actions of lead sulfide nanoparticles in different time study. Lik Sprava. 2014;3-4:114-8.
  33. 33. Liu CM, Ma JQ, Ma JQ, Sun YZ. Protective role of puerarin on lead induced alterations of the hepatic glutathione antioxidant system and hyperlipidemia in rats. Food Chem Toxicol. 2011;49:3119-27.10.1016/j.fct.2011.09.00722001170
  34. 34. Sharma V, Singh P, Pandey AK, Dhawan A. Induction of oxidative stress, DNA damage and apoptosis in mouse liver after sub-acute oral exposure to zinc oxide nanoparticles. Mutat Res. 2012;745:84-91.10.1016/j.mrgentox.2011.12.00922198329
  35. 35. Mykhaylyuk IA, Gudyma AA. Disorders of liver functional state in late period of cranialskeletal trauma and their correction by thiocetam. Vis Mor Med. 2015;4:125-9.10.11603/mcch.2410-681X.2015.v17.i2.4871
DOI: https://doi.org/10.2478/cipms-2020-0027 | Journal eISSN: 2300-6676 | Journal ISSN: 2084-980X
Language: English
Page range: 149 - 154
Submitted on: Sep 4, 2019
Accepted on: Oct 30, 2019
Published on: Sep 13, 2020
Published by: Sciendo
In partnership with: Paradigm Publishing Services
Publication frequency: 4 times per year

© 2020 Sergii Omelchuk, Vasyl Aleksiichuk, Yuri Chaikovsky, Liudmyla Sokurenko, published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.